EP0867197A2 - Implantable drug delivery device - Google Patents
Implantable drug delivery device Download PDFInfo
- Publication number
- EP0867197A2 EP0867197A2 EP98810214A EP98810214A EP0867197A2 EP 0867197 A2 EP0867197 A2 EP 0867197A2 EP 98810214 A EP98810214 A EP 98810214A EP 98810214 A EP98810214 A EP 98810214A EP 0867197 A2 EP0867197 A2 EP 0867197A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- port
- opening
- skin
- port body
- human
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/0247—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/0247—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body
- A61M2039/0261—Means for anchoring port to the body, or ports having a special shape or being made of a specific material to allow easy implantation/integration in the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/0247—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body
- A61M2039/0282—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body with implanted tubes connected to the port
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/0247—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body
- A61M2039/0288—Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body protectors, caps or covers therefor
Definitions
- the invention relates to an implantable Port body for the administration of drugs according to the Preamble of claim 1.
- a subcutaneously implantable port body is known from US-A-5 306 255.
- a subcutaneous port body lies completely under the skin and usually remains in the human body for several months or even years.
- the port chamber is located inside the port body.
- the port chamber which is completely in the human or animal body, is sealed on the skin side by a piercing membrane made of plastic, while a catheter is attached to the inside of the body, which leads to the place of distribution for medicinal products.
- the skin and membrane are pierced with a needle of an infusion set. This creates a continuous drug channel that extends from the infusion set to the point of delivery.
- a cylindrical, percutaneously implantable port body is known from patent specification EP-B-0 302 076.
- the percutaneous port body is not completely implanted in a human body, but rather is attached to the tissue in such a way that at least a certain area of the port body is not covered by skin.
- a second opening of the port body is located opposite the first opening, in the area of the port body completely surrounded by tissue.
- a catheter is connected to this opening, the end of which is located at the location within the body to which the medicament is to be transported.
- the port body consists of two screwed metal parts. Inside the port body, the port chamber, there is a pierceable membrane that separates the two openings.
- the port body is additionally anchored in the tissue by means of a base plate.
- the disadvantages of the subcutaneous port are that one neither replace the catheter nor clean it mechanically can without explanting the port.
- Another disadvantage is that the skin is always in the same place is punctured. This is painful in the short term and leads to perforation of the skin and membrane in the long term.
- the disadvantages of the percutaneous port mentioned exist in being very heavy and visible from the outside Area is very large.
- the radial grooves are designed and dimensioned to create sharp edges and corners. On these places is an optimal waxing of the Tissue cells and adequate surface cleaning not possible.
- the invention seeks to remedy this.
- the invention is based on the task of creating an inexpensive port develop, whose body-shaped housing a coherent surface and flowing transitions having.
- the port should preferably be injection molded are manufactured and are biocompatible.
- the skin has to can cling tightly to the port wall.
- the Skin waxing depth should be as uniform as possible and can be regulated by the port.
- the shape of the anchor must be designed so that in the event of a tilting moment no edges or other parts of the anchor from the Body of the patient can protrude.
- the invention solves the problem with one Port body, which has the features of claim 1.
- the advantages achieved by the invention are in essential to see that the port body is cheaper to manufacture while in use can be better cleaned by the design of the External surface is held better by the body and in case moment of tilting the skin over the anchoring surfaces rolls off.
- the choice of material, the shape and the Surface structure of the port body allow a longer implantation time.
- inside inside the human or animal body and outside outside the human or animal body.
- the Divide port body 1 into two main elements: one hollow cylindrical shaft 14 and an arranged thereon radial anchor plate 13.
- the port body 1 has two opposite openings 31a, 32 on.
- the outward opening 31a corresponds to the inside diameter of the cylindrical Port body 1.
- This opening 31a can through a lid 22, in the center of which there is a smaller opening 31b is reduced. Through this little The remaining opening 31b can be inserted into an infusion tube Interior of the port body can be pushed.
- the second, against internal opening 32 is used to arrange a Catheter 2, which the drug to be administered transported to the desired location inside the body.
- the inner wall 7 of the cylindrical port body 1 is in the Area of the cover 22 with bayonet cams 6 with integrated locking groove provided so that the lid 22, which is provided with corresponding counter elements, can be attached to the port body.
- the hollow cylindrical shaft 14 and the anchoring plate 13 become one, biologically compatible Injection molded plastic part. Between the two openings 31b, 32 there is an elastic, self-closing Membrane 21, which through the hollow cylindrical shaft 14 formed chamber 20 fills and seals.
- the cylindrical port body 14 is divided into two areas divided, an outer shaft portion 15 and an inward anchoring part 16. Between the two areas 15, 16 is a radial, protruding port rib 11 arranged.
- the shaft part 15 consists of an inert material from smooth surface structure. It ends with the outside against the outside opening 31a and against the Anchoring part 16 with the protruding port rib 11. In the skin cannot grow in this area. From the outside you can see the shaft part 15 in the implanted state clean up to the port rib 11.
- the anchoring part 16 consists of the port rib 11, one from the anchoring part 16 projecting anchoring rib 12 and the anchor plate 13. Both the port rib 11, such the anchoring rib 12 also have a peripheral one Rib margin lla, 12a.
- the port rib 11 and the Anchoring rib 12 form an intermediate one channel-shaped radial pocket 10 by the distance between the two peripheral rib edges 11a, 12a essential is narrower than the cross-sectional diameter of the radial Bag 10 itself.
- Tissue cells in the channel-shaped, radial pocket 10 wax in.
- the anchoring rib 12 can be part of the anchoring plate 13 or independent of this between the port rib 11 and the anchor plate 13 are arranged.
- the anchoring part 16 is made of a bioactive material coated and has a rough surface structure. Thereby can spread tissue in the pocket 10 and Tissue cells can adhere to the rough surface hold tight.
- tissue When tissue grows into the radial pocket 10 the tissue is wedged in the radial pocket 10 and ensures a positive connection between the fabric and the Radial pocket surface 10.
- the anchor plate 13 is radial around the Anchoring part 16 of the hollow cylindrical shaft 14 arranged.
- the anchor plate 13 has one Skin surface peripherally sloping shape, which on reminded a plate.
- the sloping shape causes the skin is affected by a tilting moment Port body 1 rolls over the anchor plate 13 and not from the edge 17 can be pierced.
- Bores 24 are made in the anchoring plate 13, which be overgrown by the surrounding tissue and thus can offer optimal support.
- the cover 22 preferably made in a skin-like color because this surface is visible to the outside.
- the whole port body can also have a skin-like color getting produced.
Abstract
Description
Die Erfindung bezieht sich auf einen implantierbaren
Portkörper zur Verabreichung von Arzneimittel gemäss dem
Oberbegriff des Anspruchs 1.The invention relates to an implantable
Port body for the administration of drugs according to the
Preamble of
Aus der Patentschrift US-A-5 306 255 ist ein subcutan
implantierbarer Portkörper bekannt. Ein subcutaner
Portkörper liegt vollkommen unter der Haut und verbleibt
normalerweise mehrere Monate oder sogar Jahre im
menschlichen Körper. Im Inneren des Portkörpers befindet
sich die Portkammer. Die sich vollständig im menschlichen
oder tierischen Körper befindende Portkammer wird
hautseitig durch eine Durchstechmembran aus Kunststoff
abgeschlossen, während gegen das Körperinnere ein Katheter
befestigt ist, welcher zum Ausschüttungsort für
Arzneimittel führt. Zur Arzneimittelverabreichung werden
Haut und Membrane mit einer Nadel eines Infusionssets
durchstochen. Dadurch entsteht ein durchgängiger
Arzneimittelkanal, welcher vom Infusionsset bis zum
Ausschüttungsort reicht.
Aus der Patentschrift EP-B-0 302 076 ist ein zylindrischer,
percutan implantierbarer Portkörper bekannt. Im Gegensatz
zum subcutanen Portkörper wird der percutane Portkörper
nicht vollständig in einen menschlichen Körper implantiert,
sondern derart im Gewebe befestigt, dass zumindest eine
bestimmte Fläche des Portkörpers nicht von Haut überdeckt
wird. Im Zentrum dieser Fläche befindet sich eine erste
Öffnung. Eine zweite Öffnung des Portkörpers befindet sich
gegenüber der ersten Öffnung, im vollständig von Gewebe
umgebenen Bereich des Portkörpers. An dieser Öffnung ist
ein Katheter angeschlossen, dessen Ende sich an demjenigen
Ort innerhalb des Körpers befindet, an den das Arzneimittel
transportiert werden soll. Der Portkörper besteht aus zwei
ineinandergeschraubten Metallteilen. Im Inneren des
Portkörpers, der Portkammer, ist eine durchstechbare
Membran angeordnet, welche die beiden Öffnungen trennt. Am
Aussenmantel des Portkörpers sind mehrere radiale Rillen,
zur seitlichen Verankerung des Ports im subcutanen
Hautgewebe angeordnet, wobei sich die äusserste Rille
direkt unter der Hautoberfläche befindet. Im Gewebe wird
der Portkörper zusätzlich mittels einer Grundplatte
verankert.A subcutaneously implantable port body is known from US-A-5 306 255. A subcutaneous port body lies completely under the skin and usually remains in the human body for several months or even years. The port chamber is located inside the port body. The port chamber, which is completely in the human or animal body, is sealed on the skin side by a piercing membrane made of plastic, while a catheter is attached to the inside of the body, which leads to the place of distribution for medicinal products. For drug administration, the skin and membrane are pierced with a needle of an infusion set. This creates a continuous drug channel that extends from the infusion set to the point of delivery.
A cylindrical, percutaneously implantable port body is known from patent specification EP-B-0 302 076. In contrast to the subcutaneous port body, the percutaneous port body is not completely implanted in a human body, but rather is attached to the tissue in such a way that at least a certain area of the port body is not covered by skin. There is a first opening in the center of this area. A second opening of the port body is located opposite the first opening, in the area of the port body completely surrounded by tissue. A catheter is connected to this opening, the end of which is located at the location within the body to which the medicament is to be transported. The port body consists of two screwed metal parts. Inside the port body, the port chamber, there is a pierceable membrane that separates the two openings. There are several radial grooves on the outer jacket of the port body for anchoring the port in the subcutaneous skin tissue, the outermost groove being located directly under the skin surface. The port body is additionally anchored in the tissue by means of a base plate.
Die Nachteile des subcutanen Ports bestehen darin, dass man den Katheter weder auswechseln, noch mechanisch reinigen kann, ohne den Port zu explantieren. Ein weiterer Nachteil besteht darin, dass die Haut immer an der gleichen Stelle durchstochen wird. Das ist kurzfristig schmerzhaft und führt längerfristig zur Perforation von Haut und Membran. Die Nachteile beim erwähnten percutanen Port bestehen darin, dass er sehr schwer und die von aussen sichtbare Fläche sehr gross ist. Zudem ist der aus Metall gefertigte Portkörper auch farblich sehr auffällig. Im montierten Zustand befindet sich ein Luftspalt zwischen der Grundplatte und dem Portkörper, welcher schwierig zu reinigen und zu sterilisieren ist. Hier besteht die Gefahr einer Infektion. Die radialen Rillen sind so angelegt und dimensioniert, dass scharfe Kanten und Ecken entstehen. An diesen Stellen ist ein optimales Einwachsen der Gewebezellen und eine ausreichende Reinigung der Oberfläche nicht möglich. Da keine geometrische Trennlinie zwischen der Hautoberfläche und der obersten Rille vorhanden ist, besteht die Gefahr, dass Körperschweiss oder Schmutz von aussen direkt in die Rillen gelangen. Es kommt im Extremfall zu einer Infektion und der Port muss explantiert werden. Ein weiterer Nachteil besteht darin, dass beim erwähnten Port die Einzelteile aus Vollmaterial in spannender Bearbeitung hergestellt werden müssen. Daher sind die Herstellkosten entsprechend hoch und jegliche Massnahme zur Gewichtsreduktion mit einem Mehraufwand verbunden. Bei den bisherigen Verankerungen besteht weiterhin die Gefahr, dass Teile der Verankerung, durch Einwirkung eines Kippmoments, aus der Haut ragen können.The disadvantages of the subcutaneous port are that one neither replace the catheter nor clean it mechanically can without explanting the port. Another disadvantage is that the skin is always in the same place is punctured. This is painful in the short term and leads to perforation of the skin and membrane in the long term. The disadvantages of the percutaneous port mentioned exist in being very heavy and visible from the outside Area is very large. In addition, the is made of metal Port body also very striking in color. In the assembled There is an air gap between the condition Base plate and the port body, which is difficult to is to be cleaned and sterilized. There is a danger here an infection. The radial grooves are designed and dimensioned to create sharp edges and corners. On these places is an optimal waxing of the Tissue cells and adequate surface cleaning not possible. Because there is no geometric dividing line between the skin surface and the top groove is present, there is a risk of body sweat or dirt from get directly into the grooves on the outside. It comes in Extreme case of infection and the port must be explanted will. Another disadvantage is that the Port mentioned the individual parts in solid material exciting machining must be produced. Therefore the manufacturing costs are correspondingly high and any Weight loss measure with additional effort connected. With the previous anchorages continue to run the risk of parts of anchoring Exposure to a tilting moment that may protrude from the skin.
Hier will die Erfindung Abhilfe verschaffen. Der Erfindung liegt die Aufgabe zugrunde, einen kostengünstigen Port zu entwickeln, dessen körpergerecht geformtes Gehäuse eine zusammenhängende Mantelfläche und fliessende Übergänge aufweist. Der Port soll vorzugsweise im Spritzgussverfahren hergestellt werden und biokompatibel sein. Die Haut muss sich fest an die Portwand klammern können. Die Einwachstiefe der Haut soll möglichst gleichmässig sein und vom Port reguliert werden können. Die Form der Verankerung muss so konzipiert werden, dass im Falle eines Kippmoments keine Kanten oder andere Teile der Verankerung aus dem Körper des Patienten ragen können.The invention seeks to remedy this. The invention is based on the task of creating an inexpensive port develop, whose body-shaped housing a coherent surface and flowing transitions having. The port should preferably be injection molded are manufactured and are biocompatible. The skin has to can cling tightly to the port wall. The Skin waxing depth should be as uniform as possible and can be regulated by the port. The shape of the anchor must be designed so that in the event of a tilting moment no edges or other parts of the anchor from the Body of the patient can protrude.
Die Erfindung löst die gestellte Aufgabe mit einem
Portkörper, welcher die Merkmale des Anspruchs 1 aufweist.The invention solves the problem with one
Port body, which has the features of
Die durch die Erfindung erreichten Vorteile sind im wesentlichen darin zu sehen, dass der Portkörper kostengünstiger herzustellen ist, während dem Gebrauch besser gereinigt werden kann, durch die Ausgestaltung der Aussenfläche vom Körper besser gehalten wird und im Falle eines Kippmoments die Haut über die Verankerungsflächen abrollt. Die Wahl des Werkstoffes, die Form und die Oberflächenstruktur des Portkörpers ermöglichen eine längere Implantationszeit.The advantages achieved by the invention are in essential to see that the port body is cheaper to manufacture while in use can be better cleaned by the design of the External surface is held better by the body and in case moment of tilting the skin over the anchoring surfaces rolls off. The choice of material, the shape and the Surface structure of the port body allow a longer implantation time.
Ein bevorzugtes Ausführungsbeispiel der Erfindung ist in den Figuren dargestellt.A preferred embodiment of the invention is in shown the figures.
Es zeigen:
Im folgenden bedeuten die Begriffe innen = innerhalb des menschlichen oder tierischen Körpers und aussen = ausserhalb des menschlichen oder tierischen Körpers.In the following, the terms inside = inside the human or animal body and outside outside the human or animal body.
Wie in den Fig. 1 und 2 dargestellt, lässt sich der
Portkörper 1 in zwei Hauptelemente einteilen: einen
hohlzylindrischen Schaft 14 und einen daran angeordneten
radialen Verankerungsteller 13.As shown in FIGS. 1 and 2, the
Divide
Der Portkörper 1 weist zwei gegenüberliegende Öffnungen
31a,32 auf. Die gegen aussen liegende Öffnung 31a
entspricht dem Innendurchmesser des zylindrischen
Portkörpers 1. Diese Öffnung 31a kann durch einen Deckel
22, in dessen Zentrum sich eine kleinere Öffnung 31b
befindet, verkleinert werden. Durch diese kleine,
verbleibende Öffnung 31b kann ein Infusionsschlauch ins
Innere des Portkörpers geschoben werden. Die zweite, gegen
innen liegende Öffnung 32 dient zur Anordnung eines
Katheters 2, welcher das zu verabreichende Arzneimittel an
den gewünschten Ort im Körperinnern transportiert.The
Die Innenwandung 7 des zylindrischen Portkörpers 1 ist im
Bereich des Deckels 22 mit Bajonettnocken 6 mit
integrierter Verriegelungsnute versehen, so dass der Deckel
22, welcher mit entsprechenden Gegenelementen versehen ist,
am Portkörper befestigt werden kann.The
Der hohlzylindrische Schaft 14 und der Verankerungsteller
13 werden aus einem einzigen, biologisch verträglichen
Kunststoffteil gespritzt. Zwischen den beiden Öffnungen
31b,32 befindet sich eine elastische, selbstschliessende
Membran 21, welche die durch den hohlzylindrischen Schaft
14 gebildete Kammer 20 ausfüllt und abdichtet.The hollow
Der zylindrische Portkörper 14 wird in zwei Bereiche
aufgeteilt, einen gegen aussen liegenden Schaftteil 15 und
einen gegen innen liegenden Verankerungsteil 16. Zwischen
den beiden Bereichen 15,16 ist eine radial verlaufende,
vorstehende Portrippe 11 angeordnet.The
Der Schaftteil 15 besteht aus einem inerten Material von
glatter Oberflächenstruktur. Er endet gegen aussen mit der
gegen aussen liegenden Öffnung 31a und gegen den
Verankerungsteil 16 mit der vorstehenden Portrippe 11. In
diesem Bereich kann die Haut nicht anwachsen. Von aussen
kann man den Schaftteil 15 im implantierten Zustand
reinigen bis zur Portrippe 11.The
Der Verankerungsteil 16 besteht aus der Portrippe 11, einer
vom Verankerungsteil 16 abstehende Verankerungsrippe 12 und
dem Verankerungsteller 13. Sowohl die Portrippe 11, wie
auch die Verankerungsrippe 12 weisen einen peripheren
Rippenrand lla,12a auf. Die Portrippe 11 und die
Verankerungsrippe 12 bilden eine dazwischenliegende
kanalförmige, radiale Tasche 10, indem der Abstand zwischen
den beiden peripheren Rippenrändern lla,12a wesentlich
enger ist, als der Querschnittdurchmesser der radialen
Tasche 10 selbst. Durch den zwischen den beiden
Rippenrändern lla,12a gebildeten Abstand können
Gewebezellen in die kanalförmige, radiale Tasche 10
einwachsen.The anchoring
Die Verankerungsrippe 12 kann Teil des Verankerungstellers
13 sein oder unabhängig von diesem zwischen der Portrippe
11 und dem Verankerungsteller 13 angeordnet werden.The anchoring
Der Verankerungsteil 16 ist mit einem bioaktiven Material
beschichtet und hat eine rauhe Oberflächenstruktur. Dadurch
kann sich Gewebe in der Tasche 10 ausbreiten und
Gewebezellen können sich an der rauhen Oberfläche
festhalten.The anchoring
Beim Einwachsen von Gewebe in die radiale Tasche 10
verkeilt sich das Gewebe in der radialen Tasche 10 und
sorgt für eine formschlüssige Verbindung Gewebe und der
Oberfläche der radialen Tasche 10.When tissue grows into the
Der Verankerungsteller 13 ist radial um den
Verankerungsteil 16 des hohlzylindrischen Schafts 14
angeordnet. Der Verankerungsteller 13 weist eine zur
Hautoberfläche peripher abfallende Form auf, welche an
einen Teller erinnert. Die abfallende Form bewirkt, dass
sich die Haut bei Einwirkung eines Kippmoments auf den
Portkörper 1 über den Verankerungsteller 13 rollt und nicht
von dessen Rand 17 durchbohrt werden kann. The
Im Verankerungsteller 13 sind Bohrungen 24 angelegt, welche
vom umliegenden Gewebe durchwachsen werden und somit
optimalen Halt bieten können.
Damit der Portdeckel 22 im implantierten Zustand geöffnet
werden kann, ist am oberen Ende der Aussenfläche des
Portschafts 15 eine Montagehilfsaussparung 9 angeordnet.
Drei solche Aussparungen 9 auf gleicher Höhe werden von
einem Spezialwerkzeug gefasst und der Deckel 22, dessen
Öffnung 31b sechskantig ausgeführt ist, wird durch eine
Drehbewegung aus der Verbindung mit dem Portkörper 14
gelöst.So that the
Bei einem percutanen Portkörper 1, wird der Deckel 22
vorzugsweise in einer hautähnliche Farbe hergestellt, da
diese Fläche gegen aussen sichtbar ist. Selbstverständlich
kann auch der ganze Portkörper in einer hautähnlichen Farbe
hergestellt werden.In the case of a
Claims (10)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH00729/97A CH692239A5 (en) | 1997-03-26 | 1997-03-26 | Port body for drug administration. |
CH72997 | 1997-03-26 | ||
CH729/97 | 1997-03-26 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0867197A2 true EP0867197A2 (en) | 1998-09-30 |
EP0867197A3 EP0867197A3 (en) | 1998-12-23 |
EP0867197B1 EP0867197B1 (en) | 2003-10-01 |
Family
ID=4193827
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98810214A Expired - Lifetime EP0867197B1 (en) | 1997-03-26 | 1998-03-13 | Implantable drug delivery device |
Country Status (9)
Country | Link |
---|---|
US (1) | US6270475B1 (en) |
EP (1) | EP0867197B1 (en) |
JP (1) | JP4030179B2 (en) |
AT (1) | ATE250955T1 (en) |
AU (1) | AU726768B2 (en) |
CA (1) | CA2233043C (en) |
CH (1) | CH692239A5 (en) |
DE (1) | DE59809760D1 (en) |
ZA (1) | ZA982512B (en) |
Cited By (7)
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WO2003020343A1 (en) | 2001-08-31 | 2003-03-13 | Disetronic Licensing Ag | Connecting device for a percutaneously implanted port and port system comprising the connecting device |
WO2003020360A1 (en) | 2001-08-31 | 2003-03-13 | Disetronic Licensing Ag | Membrane, membrane/cannula combination and connecting device |
WO2005056079A1 (en) * | 2003-12-08 | 2005-06-23 | Otto Bock Healthcare Gmbh | Implant with a skin penetration section |
DE10142637B4 (en) * | 2001-08-31 | 2009-07-09 | Disetronic Licensing Ag | Transcutaneous implant with surface structure and method for producing such an implant |
EP2616135A1 (en) * | 2010-09-17 | 2013-07-24 | Couch, Christopher John | Conical port |
EP3760273A1 (en) | 2019-07-02 | 2021-01-06 | SeraIP AG | Implantable skin penetration device |
WO2022148537A1 (en) | 2021-01-06 | 2022-07-14 | Securecell Ag | Implantable skin-piercing device |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20010051794A1 (en) * | 1997-03-26 | 2001-12-13 | Gilberto Bestetti | Port body for the administration of drugs |
US6945955B1 (en) | 1998-05-20 | 2005-09-20 | Disetronic Licensing Ag | Sensor system including a port body |
DE19822711B4 (en) * | 1998-05-20 | 2006-11-23 | Disetronic Licensing Ag | Sensor system with port body |
US7864758B1 (en) * | 2001-09-28 | 2011-01-04 | Emc Corporation | Virtualization in a storage system |
US7232429B2 (en) * | 2002-04-08 | 2007-06-19 | Boston Scientific Corporation | Medical devices |
US7570997B2 (en) | 2003-04-11 | 2009-08-04 | Cardiac Pacemakers, Inc. | Subcutaneous cardiac rhythm management with asystole prevention therapy |
US7302294B2 (en) | 2003-04-11 | 2007-11-27 | Cardiac Pacemakers, Inc. | Subcutaneous cardiac sensing and stimulation system employing blood sensor |
US7979122B2 (en) | 2003-04-11 | 2011-07-12 | Cardiac Pacemakers, Inc. | Implantable sudden cardiac death prevention device with reduced programmable feature set |
US20050240155A1 (en) * | 2004-04-27 | 2005-10-27 | Conlon Sean P | Surgically implantable injection port having a centered catheter connection tube |
EP2471573B1 (en) | 2008-04-17 | 2015-09-30 | Apollo Endosurgery, Inc. | Implantable access port device and attachment system |
US9023063B2 (en) | 2008-04-17 | 2015-05-05 | Apollo Endosurgery, Inc. | Implantable access port device having a safety cap |
US8708979B2 (en) | 2009-08-26 | 2014-04-29 | Apollo Endosurgery, Inc. | Implantable coupling device |
US8506532B2 (en) | 2009-08-26 | 2013-08-13 | Allergan, Inc. | System including access port and applicator tool |
US8715158B2 (en) | 2009-08-26 | 2014-05-06 | Apollo Endosurgery, Inc. | Implantable bottom exit port |
US8882728B2 (en) | 2010-02-10 | 2014-11-11 | Apollo Endosurgery, Inc. | Implantable injection port |
US8992415B2 (en) | 2010-04-30 | 2015-03-31 | Apollo Endosurgery, Inc. | Implantable device to protect tubing from puncture |
US20110270025A1 (en) | 2010-04-30 | 2011-11-03 | Allergan, Inc. | Remotely powered remotely adjustable gastric band system |
US20110270021A1 (en) | 2010-04-30 | 2011-11-03 | Allergan, Inc. | Electronically enhanced access port for a fluid filled implant |
US20120041258A1 (en) | 2010-08-16 | 2012-02-16 | Allergan, Inc. | Implantable access port system |
US20120065460A1 (en) | 2010-09-14 | 2012-03-15 | Greg Nitka | Implantable access port system |
US8821373B2 (en) | 2011-05-10 | 2014-09-02 | Apollo Endosurgery, Inc. | Directionless (orientation independent) needle injection port |
US8801597B2 (en) | 2011-08-25 | 2014-08-12 | Apollo Endosurgery, Inc. | Implantable access port with mesh attachment rivets |
US9199069B2 (en) | 2011-10-20 | 2015-12-01 | Apollo Endosurgery, Inc. | Implantable injection port |
US8858421B2 (en) | 2011-11-15 | 2014-10-14 | Apollo Endosurgery, Inc. | Interior needle stick guard stems for tubes |
US9089395B2 (en) | 2011-11-16 | 2015-07-28 | Appolo Endosurgery, Inc. | Pre-loaded septum for use with an access port |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0302076B1 (en) | 1986-04-18 | 1992-12-23 | LUNDGREN, Dan | Implant passageway |
US5306255A (en) | 1991-09-07 | 1994-04-26 | Hans Haindl | Portcatheter |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3783868A (en) * | 1971-05-06 | 1974-01-08 | Gulf Oil Corp | Percutaneous implant |
US4183357A (en) * | 1976-08-02 | 1980-01-15 | Bentley Laboratories, Inc. | Chronic transcutaneous implant assembly for enterostomies |
US4092983A (en) * | 1977-01-31 | 1978-06-06 | General Atomic Company | Blood access device |
GB2050175B (en) * | 1977-07-07 | 1982-07-14 | Bentley Lab | A traumatic valving mechanism |
US4321914A (en) * | 1980-04-22 | 1982-03-30 | W. L. Gore & Associates, Inc. | Percutaneous conduit having PTFE skirt |
US4578063A (en) * | 1984-09-14 | 1986-03-25 | W. L. Gore & Assoc., Inc. | Central venous catheter |
DE3742263A1 (en) | 1987-12-12 | 1989-06-22 | Plastik Fuer Die Medizin Pfm | METHOD AND DEVICE FOR PERMANENTLY TAKING BLOOD FROM ANIMALS |
SE465910B (en) * | 1988-01-28 | 1991-11-18 | Jan Axel Svensson | DEVICE FOR CONNECTING CATHETRES IN A SKIN REVIEW |
US4955861A (en) | 1988-04-21 | 1990-09-11 | Therex Corp. | Dual access infusion and monitoring system |
US5242415A (en) * | 1992-08-14 | 1993-09-07 | L-Vad Technology, Inc. | Percutaneous access device |
US5741234A (en) * | 1996-07-16 | 1998-04-21 | Aboul-Hosn; Walid Nagib | Anatomical cavity access sealing condit |
-
1997
- 1997-03-26 CH CH00729/97A patent/CH692239A5/en not_active IP Right Cessation
-
1998
- 1998-03-13 DE DE59809760T patent/DE59809760D1/en not_active Expired - Lifetime
- 1998-03-13 AT AT98810214T patent/ATE250955T1/en not_active IP Right Cessation
- 1998-03-13 EP EP98810214A patent/EP0867197B1/en not_active Expired - Lifetime
- 1998-03-25 CA CA002233043A patent/CA2233043C/en not_active Expired - Fee Related
- 1998-03-25 AU AU59533/98A patent/AU726768B2/en not_active Ceased
- 1998-03-25 ZA ZA982512A patent/ZA982512B/en unknown
- 1998-03-26 US US09/048,682 patent/US6270475B1/en not_active Expired - Lifetime
- 1998-03-26 JP JP07868998A patent/JP4030179B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0302076B1 (en) | 1986-04-18 | 1992-12-23 | LUNDGREN, Dan | Implant passageway |
US5306255A (en) | 1991-09-07 | 1994-04-26 | Hans Haindl | Portcatheter |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003020343A1 (en) | 2001-08-31 | 2003-03-13 | Disetronic Licensing Ag | Connecting device for a percutaneously implanted port and port system comprising the connecting device |
WO2003020360A1 (en) | 2001-08-31 | 2003-03-13 | Disetronic Licensing Ag | Membrane, membrane/cannula combination and connecting device |
DE10142637B4 (en) * | 2001-08-31 | 2009-07-09 | Disetronic Licensing Ag | Transcutaneous implant with surface structure and method for producing such an implant |
WO2005056079A1 (en) * | 2003-12-08 | 2005-06-23 | Otto Bock Healthcare Gmbh | Implant with a skin penetration section |
EP2616135A1 (en) * | 2010-09-17 | 2013-07-24 | Couch, Christopher John | Conical port |
EP2616135A4 (en) * | 2010-09-17 | 2014-07-23 | Couch Christopher John | Conical port |
EP3760273A1 (en) | 2019-07-02 | 2021-01-06 | SeraIP AG | Implantable skin penetration device |
WO2022148537A1 (en) | 2021-01-06 | 2022-07-14 | Securecell Ag | Implantable skin-piercing device |
Also Published As
Publication number | Publication date |
---|---|
EP0867197B1 (en) | 2003-10-01 |
AU5953398A (en) | 1998-10-01 |
AU726768B2 (en) | 2000-11-23 |
EP0867197A3 (en) | 1998-12-23 |
ZA982512B (en) | 1998-09-30 |
CA2233043A1 (en) | 1998-09-26 |
JPH10290840A (en) | 1998-11-04 |
US6270475B1 (en) | 2001-08-07 |
ATE250955T1 (en) | 2003-10-15 |
CA2233043C (en) | 2007-09-18 |
CH692239A5 (en) | 2002-04-15 |
JP4030179B2 (en) | 2008-01-09 |
DE59809760D1 (en) | 2003-11-06 |
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